A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4020369



Internal ID22082000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:163587561..163595782hg38UCSC Ensembl
Outerchr5:163582972..163595977hg38UCSC Ensembl
Innerchr5:163014567..163022788hg19UCSC Ensembl
Outerchr5:163009978..163022983hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3813006
hg1913006
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156404
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4020369
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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